A255
A-77636 hydrochloride hydrate
≥98% (HPLC), solid
别名:
(−)-(1R,3S)-3-Adamantyl-1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-1H-2-benzopyran hydrochloride hydrate
质量水平
方案
≥98% (HPLC)
表单
solid
储存条件
desiccated
protect from light
颜色
white to off-white
溶解性
H2O: >10 mg/mL
储存温度
−20°C
SMILES字符串
O.Cl.NC[C@@H]1O[C@@H](Cc2c(O)c(O)ccc12)C34CC5CC(CC(C5)C3)C4
InChI
1S/C20H27NO3.ClH.H2O/c21-10-17-14-1-2-16(22)19(23)15(14)6-18(24-17)20-7-11-3-12(8-20)5-13(4-11)9-20;;/h1-2,11-13,17-18,22-23H,3-10,21H2;1H;1H2/t11?,12?,13?,17-,18-,20?;;/m0../s1
InChI key
KNACNUUSUYTFDY-LIWDBWMRSA-N
基因信息
human ... DRD1(1812)
相关类别
生化/生理作用
Potent, orally active D1 dopamine receptor agonist.
特点和优势
This compound is featured on the Dopamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
法律信息
Manufactured and sold under exclusive license from Abbott Laboratories.
免责声明
Hygroscopic, photosensitive, and oxygen-sensitive. Solutions should be freshly prepared.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Jessica P Ryman-Rasmussen et al.
Neuropharmacology, 52(2), 562-575 (2006-10-28)
Recently, we demonstrated that D(1) agonists can cause functionally selective effects when the endpoints of receptor internalization and adenylate cyclase activation are compared. The present study was designed to probe the phenomenon of functional selectivity at the D(1) receptor further
J W Kebabian et al.
European journal of pharmacology, 229(2-3), 203-209 (1992-12-15)
A-77636, ((1R,3S) 3-(1'-adamantyl)-1-aminomethyl-3,4-dihydro-5,6-dihydroxy-1H-2-benz opyran hydrochloride), is a selective dopamine D1 receptor agonist. In a battery of receptor binding assays, A-77636 shows the highest affinity (pKi = 7.40 +/- 0.09; Ki = 39.8 nM) for the dopamine D1 receptor. A-77636 is
E Acquas et al.
Journal of neurochemistry, 70(3), 1088-1093 (1998-03-07)
This study examined the effects of different levels of acetylcholinesterase (AChE) inhibition on dopaminergic regulation of striatal acetylcholine (ACh) release as estimated by in vivo brain microdialysis. Systemic administration of d-amphetamine (2 or 10 mg/kg) increased the striatal output of
Ales Stuchlik et al.
Behavioural brain research, 172(2), 250-255 (2006-06-20)
Central dopamine neurotransmission is implicated in several physiological and pathophysiological neural processes. In the past years, attention was paid to the role of dopaminergic signaling in the cognitive processes. In the present study, we investigate role of dopamine D1 receptors
D Wirtshafter
Synapse (New York, N.Y.), 28(2), 154-159 (1998-02-05)
Systemic injections of the selective, full, D1 agonists A-77636 and SKF-82958 induced pronounced Fos-like immunoreactivity in the islands of Calleja in the olfactory tubercle of intact rats. Fos expression in this region could also be induced by injections of the
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